A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836922



Internal ID22611857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9824894..9829755hg38UCSC Ensembl
chr3:9866578..9871439hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384862
hg194862
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497524
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836922
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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